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Evading anti-angiogenic therapy: resistance to anti-angiogenic therapy in solid tumors

机译:规避抗血管生成疗法:对实体瘤抗血管生成疗法的抵抗

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摘要

Vascular endothelial growth factor (VEGF) dependent tumor angiogenesis is an essential step for the initiation and promotion of tumor progression. The hypothesis that VEGF-driven tumor angiogenesis is necessary and sufficient for metastatic progression of the tumor, has been the major premise of the use of anti-VEGF therapy for decades. While the success of anti-VEGF therapy in solid tumors has led to the success of knowledge-based-therapies over the past several years, failures of this therapeutic approach due to the development of inherent/acquired resistance has led to the increased understanding of VEGF-independent angiogenesis. Today, tumor-angiogenesis is not a synonymous term to VEGF-dependent function. The extensive study of VEGF-independent angiogenesis has revealed several key factors responsible for this phenomenon including the role of myeloid cells, and the contribution of entirely new phenomenon like vascular mimicry. In this review, we will present the cellular and molecular factors related to the development of anti-angiogenic resistance following anti-VEGF therapy in different solid tumors.
机译:血管内皮生长因子(VEGF)依赖性肿瘤血管生成是引发和促进肿瘤进展的重要步骤。数十年来,一直认为VEGF驱动的肿瘤血管生成对于肿瘤的转移进程是必要和充分的,这一直是使用抗VEGF疗法的主要前提。尽管在过去的几年中,抗VEGF治疗在实体瘤中的成功已导致基于知识的疗法的成功,但由于固有/获得性耐药性的发展,这种治疗方法的失败导致对VEGF的了解增加非依赖性血管生成。如今,肿瘤血管生成已不是VEGF依赖功能的同义词。对VEGF非依赖性血管生成的广泛研究揭示了造成这种现象的几个关键因素,包括髓样细胞的作用以及像血管拟态一样的全新现象的贡献。在这篇综述中,我们将介绍在不同实体瘤中抗VEGF治疗后与抗血管生成抗性发展有关的细胞和分子因素。

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